Rubidium chloride is the chemical compound with the formula RbCl. This alkali metal halide salt is composed of rubidium and chlorine, and finds diverse uses ranging from electrochemistry to molecular biology.
In its gas phase, RbCl is diatomic with a bond length estimated at 2.7868 Å. This distance increases to 3.285 Å for cubic RbCl, reflecting the higher coordination number of the ions in the solid phase.
Depending on conditions, solid RbCl exists in one of three arrangements or polymorphs as determined with holographic imaging:
The sodium chloride (NaCl) polymorph is most common. A cubic close-packed arrangement of chloride anions with rubidium cations filling the octahedral holes describes this polymorph. Both ions are six-coordinate in this arrangement. The lattice energy of this polymorph is only 3.2 kJ/mol less than the following structure's.
At high temperature and pressure, RbCl adopts the caesium chloride (CsCl) structure (NaCl and KCl undergo the same structural change at high pressures). Here, the chloride ions form a simple cubic arrangement with chloride anions occupying the vertices of a cube surrounding a central Rb+. This is RbCl's densest packing motif. Because a cube has eight vertices, both ions' coordination numbers equal eight. This is RbCl's highest possible coordination number. Therefore, according to the radius ratio rule, cations in this polymorph will reach their largest apparent radius because the anion-cation distances are greatest.
The sphalerite polymorph of rubidium chloride has not been observed experimentally. This is consistent with the theory; the lattice energy is predicted to be nearly 40.0 kJ/mol smaller in magnitude than those of the preceding structures.
The most common preparation of pure rubidium chloride involves the reaction of its hydroxide with hydrochloric acid, followed by recrystallization:
RbOH + HCl → RbCl + H2O
Because RbCl is hygroscopic, it must be protected from atmospheric moisture, e.g. using a desiccator. RbCl is primarily used in laboratories.
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Covers the formation, classes, and properties of intermetallic compounds, including specific examples like titanium aluminides, nickel aluminides, and iron aluminides.
Caesium chloride or cesium chloride is the inorganic compound with the formula CsCl. This colorless salt is an important source of caesium ions in a variety of niche applications. Its crystal structure forms a major structural type where each caesium ion is coordinated by 8 chloride ions. Caesium chloride dissolves in water. CsCl changes to NaCl structure on heating. Caesium chloride occurs naturally as impurities in carnallite (up to 0.002%), sylvite and kainite.
In crystallography, the cubic (or isometric) crystal system is a crystal system where the unit cell is in the shape of a cube. This is one of the most common and simplest shapes found in crystals and minerals. There are three main varieties of these crystals: Primitive cubic (abbreviated cP and alternatively called simple cubic) Body-centered cubic (abbreviated cI or bcc) Face-centered cubic (abbreviated cF or fcc) Note: the term fcc is often used in synonym for the cubic close-packed or ccp structure occurring in metals.
Potassium chloride (KCl, or potassium salt) is a metal halide salt composed of potassium and chlorine. It is odorless and has a white or colorless vitreous crystal appearance. The solid dissolves readily in water, and its solutions have a salt-like taste. Potassium chloride can be obtained from ancient dried lake deposits. KCl is used as a fertilizer, in medicine, in scientific applications, domestic water softeners (as a substitute for sodium chloride salt), and in food processing, where it may be known as E number additive E508.
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